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If you wanted to make a circle graph of the data, what additional category would you have to include so that the circle graph would not be misleading. 27 (A) Complex skull fracture. 524 0. The characteristic, Chapter 3 Tumors 21 Associated with breast carcinoma May express progesterone estrogen receptors Most arise proximal to meninges from arach- noidal cap cells; falx cerebri is single most common site of origin Rarely arise in unusual sites such as intraventric- ular region, head and neck, ear, nasopharynx, or lung Most are slow growing and present with signs and symptoms related to compression of adjacent structures Grossly, most are well circumscribed; compress adjacent parenchyma May invade skull and produce hyperostosis Gross appearance may be variable, depending on histological type A variety of benign histological subtypes have been defined (WHO grade I tumors) Meningothelial (syncytial)-cells arranged in lobules divided by collagenous septae, whor- ling of cells around vessels or psammoma bodies (calcifications), eosinophilic cyto- plasmic protrusions into the nuclei prominent (nuclear pseudoinclusions) Fibrous (fibroblastic)-spindle cells with abundant collagen or reticulin between cells Transitional (mixed)-features of both meningothelial and fibrous types Psammomatous-abundant calcifications Angiomatous-marked by prominent vascu- lature, not to be confused with hemangioper- icytoma or hemangioblastoma Microcystic-loose, mucinous background Secretory (pseudopsammomatous)- formation of intracellular lumina containing PAS positive, eosinophilic material Lymphoplasmacyte rich-marked by exten- sive chronic inflammation Metaplastic-demonstrates mesenchymal differentiation (bone, cartilage, fat) WHO grade I tumors marked by low rate of cell proliferation Immunohistochemistry: most EMA and vimentin positive; variable positivity with S-100 protein and cytokeratins Electron microscopy shows prominent interdigi- tated cell processes and desmosomal junctions May be induced by prior radiation Most common cytogenetic abnormality is dele- tion of chromosome 22q; other less frequent abnormalities are deletionloss on 1p, 6q, 9q, 10q, 14q, 17p, and 18q Potentially curable with gross total resection, a subset does recur over time B.

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ASSAY Dissolve 0. McCaughan, D. Dev Neuroscience 1997; 19:27-32. 25; }; datablock ParticleEmitterData(CrossbowExplosionSmokeEmitter) { ejectionPeriodMS 10; periodVarianceMS 0; ejectionVelocity 4; velocityVariance 0.

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